K14N (p.Lys14Asn) variant of ANKRD1 (Q15327)
K14N (p.Lys14Asn) in ANKRD1 (Q15327) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
K14N (p.Lys14Asn) variant details
- p.Lys14Asn
- NCI-TCGA Cosmic COSV6331
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.309
- REVEL 0.20
- CADD 24.10
- PolyPhen-2 0.74
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available